Sweta Iyer

840 total citations
17 papers, 627 citations indexed

About

Sweta Iyer is a scholar working on Molecular Biology, Cell Biology and Ecology. According to data from OpenAlex, Sweta Iyer has authored 17 papers receiving a total of 627 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 3 papers in Cell Biology and 2 papers in Ecology. Recurrent topics in Sweta Iyer's work include Cell death mechanisms and regulation (12 papers), RNA Interference and Gene Delivery (8 papers) and Mitochondrial Function and Pathology (6 papers). Sweta Iyer is often cited by papers focused on Cell death mechanisms and regulation (12 papers), RNA Interference and Gene Delivery (8 papers) and Mitochondrial Function and Pathology (6 papers). Sweta Iyer collaborates with scholars based in Australia, India and United States. Sweta Iyer's co-authors include Ruth M. Kluck, Grant Dewson, Rachel T. Uren, Brian J. Smith, Dana Westphal, Marie Ménard, Ray C. Bartolo, Amber E. Alsop, Jerry M. Adams and Peter E. Czabotar and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Molecular Cell.

In The Last Decade

Sweta Iyer

17 papers receiving 624 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sweta Iyer Australia 12 507 81 80 54 52 17 627
Hetal Brahmbhatt United States 8 417 0.8× 72 0.9× 61 0.8× 36 0.7× 70 1.3× 17 563
Emily E. Fink United States 13 438 0.9× 83 1.0× 37 0.5× 64 1.2× 44 0.8× 18 549
Tamara Kanashova Germany 9 333 0.7× 63 0.8× 53 0.7× 59 1.1× 31 0.6× 10 511
Pey Yee Lee Malaysia 11 360 0.7× 65 0.8× 43 0.5× 49 0.9× 20 0.4× 18 542
Marguerite L. Davis United States 4 701 1.4× 120 1.5× 102 1.3× 40 0.7× 79 1.5× 5 810
Gillian L. Dornan Canada 11 450 0.9× 48 0.6× 80 1.0× 39 0.7× 36 0.7× 15 599
Ulrich Goldmann Austria 7 261 0.5× 117 1.4× 66 0.8× 42 0.8× 30 0.6× 10 443
Michelina Festa Italy 11 323 0.6× 54 0.7× 28 0.3× 31 0.6× 35 0.7× 14 416
Litong Du United States 8 393 0.8× 76 0.9× 64 0.8× 26 0.5× 23 0.4× 9 491
Lisa J. Neilson United Kingdom 12 322 0.6× 109 1.3× 60 0.8× 123 2.3× 38 0.7× 21 595

Countries citing papers authored by Sweta Iyer

Since Specialization
Citations

This map shows the geographic impact of Sweta Iyer's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sweta Iyer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sweta Iyer more than expected).

Fields of papers citing papers by Sweta Iyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sweta Iyer. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sweta Iyer. The network helps show where Sweta Iyer may publish in the future.

Co-authorship network of co-authors of Sweta Iyer

This figure shows the co-authorship network connecting the top 25 collaborators of Sweta Iyer. A scholar is included among the top collaborators of Sweta Iyer based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sweta Iyer. Sweta Iyer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Iyer, Sweta, Agnes W. Wong, Ahmad Z. Wardak, et al.. (2024). A novel inhibitory BAK antibody enables assessment of non-activated BAK in cancer cells. Cell Death and Differentiation. 31(6). 711–721. 1 indexed citations
2.
Iyer, Sweta, et al.. (2024). Spatial prioritization of dugong habitats in India can contribute towards achieving the 30 × 30 global biodiversity target. Scientific Reports. 14(1). 13984–13984. 1 indexed citations
3.
Iyer, Sweta, et al.. (2022). Understanding dietary differences in Indian dugongs through opportunistic gut sampling of stranded individuals. Current Science. 123(10). 1259–1259. 1 indexed citations
4.
Robin, A.Y., Michelle S. Miller, Sweta Iyer, et al.. (2022). Structure of the BAK-activating antibody 7D10 bound to BAK reveals an unexpected role for the α1-α2 loop in BAK activation. Cell Death and Differentiation. 29(9). 1757–1768. 6 indexed citations
5.
Birkinshaw, Richard W., Sweta Iyer, Daisy Lio, et al.. (2021). Structure of detergent-activated BAK dimers derived from the inert monomer. Molecular Cell. 81(10). 2123–2134.e5. 27 indexed citations
6.
Iyer, Sweta, Rachel T. Uren, Michael A. Dengler, et al.. (2020). Robust autoactivation for apoptosis by BAK but not BAX highlights BAK as an important therapeutic target. Cell Death and Disease. 11(4). 268–268. 28 indexed citations
7.
Hockings, Colin, Sweta Iyer, Rachel T. Uren, & Ruth M. Kluck. (2019). Avoiding adsorption of Bcl-2 proteins to plasticware is important for accurate quantitation. Cell Death and Differentiation. 26(5). 794–795. 3 indexed citations
8.
Dengler, Michael A., A.Y. Robin, Leonie Gibson, et al.. (2019). BAX Activation: Mutations Near Its Proposed Non-canonical BH3 Binding Site Reveal Allosteric Changes Controlling Mitochondrial Association. Cell Reports. 27(2). 359–373.e6. 40 indexed citations
9.
Robin, A.Y., Sweta Iyer, Richard W. Birkinshaw, et al.. (2018). Ensemble Properties of Bax Determine Its Function. Structure. 26(10). 1346–1359.e5. 36 indexed citations
10.
Iyer, Sweta, Rachel T. Uren, & Ruth M. Kluck. (2018). Probing BAK and BAX Activation and Pore Assembly with Cytochrome c Release, Limited Proteolysis, and Oxidant-Induced Linkage. Methods in molecular biology. 1877. 201–216. 13 indexed citations
11.
Uren, Rachel T., Martin O’Hely, Sweta Iyer, et al.. (2017). Disordered clusters of Bak dimers rupture mitochondria during apoptosis. eLife. 6. 82 indexed citations
12.
Uren, Rachel T., Sweta Iyer, & Ruth M. Kluck. (2017). Pore formation by dimeric Bak and Bax: an unusual pore?. Philosophical Transactions of the Royal Society B Biological Sciences. 372(1726). 20160218–20160218. 64 indexed citations
13.
Brasacchio, Daniella, Amber E. Alsop, Tahereh Noori, et al.. (2017). Epigenetic control of mitochondrial cell death through PACS1-mediated regulation of BAX/BAK oligomerization. Cell Death and Differentiation. 24(6). 961–970. 36 indexed citations
14.
Iyer, Sweta, Khatira Anwari, Amber E. Alsop, et al.. (2016). Identification of an activation site in Bak and mitochondrial Bax triggered by antibodies. Nature Communications. 7(1). 11734–11734. 47 indexed citations
15.
Iyer, Sweta, Dana Westphal, Khatira Anwari, et al.. (2015). Bak apoptotic pores involve a flexible C-terminal region and juxtaposition of the C-terminal transmembrane domains. Cell Death and Differentiation. 22(10). 1665–1675. 50 indexed citations
16.
Westphal, Dana, Grant Dewson, Marie Ménard, et al.. (2014). Apoptotic pore formation is associated with in-plane insertion of Bak or Bax central helices into the mitochondrial outer membrane. Proceedings of the National Academy of Sciences. 111(39). E4076–85. 91 indexed citations
17.
Ma, Stephen, Thanh Ngoc Nguyen, Iris K. L. Tan, et al.. (2014). Bax targets mitochondria by distinct mechanisms before or during apoptotic cell death: a requirement for VDAC2 or Bak for efficient Bax apoptotic function. Cell Death and Differentiation. 21(12). 1925–1935. 101 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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